bioRxiv Science⌕ Search

Biology subjects

Cho, W.-K.

Publications and source records attributed to Cho, W.-K..

3 recordsLinked to original sources

Topology of gene regulatory compartments relative to the nuclear matrix

Summary ParagraphInside the nucleus, there are special compartments with characterized functions, some of which are involved in gene expression1. These compartments include transcriptional condensates and nuclear speckles, which contain factors required for transcription and splicing, respectively. While the characteristics of these intranuclear compartments were extensively investigated, spatial relationship between them is yet unclear. Meanwhile, RNA-protein structural network named the nuclear matrix has been observed inside the nucleus and suggested as a framework for the spatial segregation of the intranuclear space2-6. However, concept of the nuclear matrix was not widely accepted due to its lack of in vivo evidence7. Here, we report visualization of the nuclear matrix and intranuclear compartments using super-resolution fluorescence microscopy. We found the nuclear matrix is dynamic in live cells and easily disrupted upon transcription inhibition. Remarkably, we observed an orderly layered distribution of transcriptional condensates and nuclear speckles relative to the nuclear matrix. We also observed a separation of chromosome territories from transcriptional condensates and nuclear speckles by the nuclear matrix. Based on our findings, we propose a topological model for the regulation of transcription across the nuclear matrix.

cell biology↗

qSR: A software for quantitative analysis of single molecule and super-resolution data

Single-molecule based super-resolution microscopy (Betzig et al., 2006; Hess et al., 2006; Rust et al., 2006) provides insight into the spatiotemporal organization and dynamics of biomolecules at the length scale of ten to hundreds of nanometers, which is most relevant to protein clustering in a broad range of cellular processes. A series of quantitative analysis approaches have been developed to infer the characteristic size of protein clustering via pair correlation analysis (Sengupta et al., 2013; Sengupta et al., 2011; Veatch et al., 2012) or to merge multiple blinking localizations from single fluorophores (Annibale et al., 2011), to identify clusters based on density of detections (Ester, 1996), and to measure temporal dynamics of protein clustering in living cells (Cho et al., 2016a; ...

biophysics↗

Cell-cycle dependent organization and dynamics of RNA Polymerase I in live human cells

RNA Polymerase I (Pol I) is responsible for over 60% of transcriptional output in human cells, yet basic questions concerning the spatial and temporal organization of the polymerase remain unanswered. Here we investigate how mammalian cells rely on Pol I organization throughout the cell cycle to balance different needs, from complete transcription shut down to massive increase in protein synthesis (and thus ribosomal RNA synthesis) before cell division. In contrast to our previous reports on RNA Polymerase II, Pol I clusters are stable with active transcription, and the presence of transient Pol I clusters correlates with inactive ribosomal transcription. Our results suggest that both stable and transient populations Pol I clusters co-exist in individual living cells, and their relative fraction may directly reflect the global gene expression need of the cell.

biophysics↗